Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:106112477-106112660 | Common:1; Rare:74 | ||||
chr7:106284885-106285353 | Common:4; Rare:188 | ||||
chr7:106661152-106661273 | Common:1; Rare:17 | ||||
chr7:107563873-107564001 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
chr7:107744053-107744164 | Rare:37 | ||||
chr7:108526099-108526411 | Common:5; Rare:101 | ||||
chr7:108569566-108570040 | Common:3; Rare:168 | ||||
chr7:112206392-112206719 | Common:1; Rare:109 | ||||
chr7:116524834-116525092 | Rare:76 | ||||
chr7:116525613-116525786 | Rare:36 | ||||
chr7:116526224-116526608 | Common:2; Rare:106; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr7:118183965-118184179 | Common:1; Rare:79 | ||||
chr7:122144229-122144437 | Common:1; Rare:41 | ||||
chr7:123748912-123749229 | Common:3; Rare:111 | ||||
chr7:124929851-124929873 | Common:1; Rare:4 |